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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 11721 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepHSG576
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Backbone manufacturersee NCBI D88215
- Backbone size w/o insert (bp) 3475
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Vector typeBacterial Expression
Growth in Bacteria
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Bacterial Resistance(s)Chloramphenicol, 25 μg/mL
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Growth Temperature30°C
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Growth Strain(s)JS200
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Growth instructionsGrow at 30oC in LB in JS200 cells (polA recA718). The cells need to be kept in exponential phase (do not let the culture reach saturation)!
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Copy numberLow Copy
Gene/Insert
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Gene/Insert nameDNA polymerase I
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Alt namePolI
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Alt namePolA
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SpeciesE. coli
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Insert Size (bp)2787
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Mutationwild-type
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Entrez GenepolA (a.k.a. b3863, ECK3855, JW3835, resA)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site HindIII (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer m13 reverse primer
- 3′ sequencing primer m13 forward 20 primer (Common Sequencing Primers)
Resource Information
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Supplemental Documents
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
Control for random mutagenesis experiments. See attached mutagenesis protocol provided by depositing scientist.
Please note that this plasmid may require a unique bacterial strain, so make sure to confirm that you can also obtain the appropriate growth strain. Please contact us at [email protected] or contact our distributors if you have any questions.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
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For your Materials & Methods section:
pWT PolI was a gift from Lawrence Loeb (Addgene plasmid # 11721 ; http://n2t.net/addgene:11721 ; RRID:Addgene_11721) -
For your References section:
Targeted gene evolution in Escherichia coli using a highly error-prone DNA polymerase I. Camps M, Naukkarinen J, Johnson BP, Loeb LA. Proc Natl Acad Sci U S A. 2003 Aug 19. 100(17):9727-32. 10.1073/pnas.1333928100 PubMed 12909725